Gilles David

2.4k total citations · 2 hit papers
15 papers, 1.9k citations indexed

About

Gilles David is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Gilles David has authored 15 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 10 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Gilles David's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (10 papers) and DNA Repair Mechanisms (4 papers). Gilles David is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (10 papers) and DNA Repair Mechanisms (4 papers). Gilles David collaborates with scholars based in France, United Kingdom and United States. Gilles David's co-authors include Alexis Brice, Giovanni Stévanin, Yves Agid, Géraldine Cancel‐Tassin, Jean‐Louis Mandel, Georges Imbert, C. R. Weber, Frédéric Saudou, Paola Giunti and Nicholas Wood and has published in prestigious journals such as Nature, Nature Genetics and Neurology.

In The Last Decade

Gilles David

15 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

1997 599 citations Gilles David, Nacer Abbas et al. Nature Genetics profile →
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

1995 540 citations Yvon Trottier, Yves Lutz et al. Nature profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Gilles David France	11	1.8k	1.7k	598	127	107	15	1.9k
Astrid Lunkes Germany	12	1.5k 0.8×	1.4k 0.8×	648 1.1×	99 0.8×	67 0.6×	18	1.8k
Olivier Didierjean France	10	1.5k 0.8×	1.4k 0.8×	697 1.2×	80 0.6×	69 0.6×	13	1.7k
Francesca Cavalcanti Italy	20	1.0k 0.6×	974 0.6×	408 0.7×	113 0.9×	50 0.5×	43	1.3k
A. Ishikawa Japan	4	964 0.5×	912 0.5×	387 0.6×	184 1.4×	35 0.3×	7	1.1k
Kellie Benzow United States	11	1.1k 0.6×	1.1k 0.6×	357 0.6×	146 1.1×	31 0.3×	18	1.3k
Imma Castaldo Italy	18	723 0.4×	820 0.5×	307 0.5×	70 0.6×	44 0.4×	27	973
Maria do Carmo Costa United States	22	988 0.6×	1.1k 0.6×	298 0.5×	82 0.6×	30 0.3×	37	1.3k
Mary L. Franz United States	12	970 0.6×	818 0.5×	493 0.8×	94 0.7×	19 0.2×	16	1.1k
Thorsten Schulte Germany	11	882 0.5×	679 0.4×	565 0.9×	46 0.4×	27 0.3×	15	1.1k
Isabelle Le Ber France	13	705 0.4×	654 0.4×	346 0.6×	79 0.6×	32 0.3×	18	908

Countries citing papers authored by Gilles David

Since Specialization

Citations

This map shows the geographic impact of Gilles David's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gilles David with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gilles David more than expected).

Fields of papers citing papers by Gilles David

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gilles David. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gilles David. The network helps show where Gilles David may publish in the future.

Co-authorship network of co-authors of Gilles David

This figure shows the co-authorship network connecting the top 25 collaborators of Gilles David. A scholar is included among the top collaborators of Gilles David based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gilles David. Gilles David is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

David, Gilles. (2012). Contribution à l'étude du slack organisationnel : le cas des dépenses d'investissements dans une grande entreprise industrielle. La Revue des sciences de gestion/La Revue des sciences de gestion, Direction et gestion. n° 254(2). 59–68. 1 indexed citations

David, Gilles. (2005). Nécessité et efficacité d’une approche intégrée dans le traitement de l’inceste. Service social. 36(2-3). 350–368. 2 indexed citations

David, Gilles, et al.. (2004). The Role of Regional Industry Clusters in Urban Economic Development: An Analysis of Process and Performance. 4 indexed citations

Miller, M. A., et al.. (2002). HACT Flight Control System (HFCS) Control Law Overview. 5 indexed citations

Giunti, Paola, Giovanni Stévanin, Paul Worth, et al.. (1999). Molecular and Clinical Study of 18 Families with ADCA Type II: Evidence for Genetic Heterogeneity and De Novo Mutation. The American Journal of Human Genetics. 64(6). 1594–1603. 76 indexed citations

Stévanin, Giovanni, Gilles David, Alexandra Dürr, et al.. (1999). Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG). European Journal of Human Genetics. 7(8). 889–896. 28 indexed citations

Stévanin, Giovanni, Paola Giunti, Gilles David, et al.. (1998). De Novo Expansion of Intermediate Alleles in Spinocerebellar Ataxia 7. Human Molecular Genetics. 7(11). 1809–1813. 76 indexed citations

David, Gilles. (1998). Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). Human Molecular Genetics. 7(2). 165–170. 208 indexed citations

David, Gilles, Nacer Abbas, Giovanni Stévanin, et al.. (1997). Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nature Genetics. 17(1). 65–70. 599 indexed citations breakdown →

10.

Martin, Jean‐Jacques, Gilles David, Nicole Van Regemorter, et al.. (1997). Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1. Human Genetics. 99(2). 225–232. 19 indexed citations

11.

Stévanin, Giovanni, Alexandra Dürr, Gilles David, et al.. (1997). Clinical and molecular features of spinocerebellar ataxia type 6. Neurology. 49(5). 1243–1246. 102 indexed citations

12.

David, Gilles, Paola Giunti, N. Abbas, et al.. (1996). The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.. PubMed. 59(6). 1328–36. 52 indexed citations

13.

Lindblad, K, M L Savontaus, Giovanni Stévanin, et al.. (1996). An expanded CAG repeat sequence in spinocerebellar ataxia type 7.. Genome Research. 6(10). 965–971. 85 indexed citations

14.

Benomar, Ali, Giovanni Stévanin, Géraldine Cancel‐Tassin, et al.. (1995). The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1. Nature Genetics. 10(1). 84–88. 126 indexed citations

15.

Trottier, Yvon, Yves Lutz, Giovanni Stévanin, et al.. (1995). Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature. 378(6555). 403–406. 540 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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